B L O O D C O M P O N E N T S
The use of cryopreserved platelets in a trauma-induced
hemorrhage model
Derek J.B. Kleinveld
1,2,3|
Pieter H. Sloos
1,2|
Femke Noorman
4|
M. Adrie W. Maas
1,2|
Jesper Kers
5,6,7,8|
Tim W.H. Rijnhout
9,10|
Margreet Zoodsma
4|
Rigo Hoencamp
9,10,11,12|
Markus W. Hollmann
2,13|
Nicole P. Juffermans
2,141Department of Intensive Care, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands
2Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands 3Department of Trauma Surgery, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands
4Military Blood Bank, Utrecht, The Netherlands
5Department of Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands 6Department of Pathology, Leiden UMC, University of Leiden, Leiden, The Netherlands
7Van 't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam, Amsterdam, The Netherlands
8Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology & Harvard University, Cambridge, Massachusetts, USA 9Department of Surgery, Alrijne Medical Center, Leiderdorp, The Netherlands
10Trauma Research Unit Department of Surgery, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands 11Department of Surgery, Leiden UMC, University of Leiden, Leiden, The Netherlands
12Defense Healthcare Organization, Ministry of Defense, Utrecht, The Netherlands
13Department of Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands 14Department of Intensive Care Medicine, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands
Correspondence
Derek J.B. Kleinveld, Amsterdam UMC, University of Amsterdam, Intensive Care, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Email: d.j.kleinveld@amsterdamumc.nl Funding information
Dutch Ministry of Defense; Stichting Ziektekostenverzekering Krijgsmacht (SZVK)
Abstract
Background: Cryopreserved platelet products can be stored for years and are mainly used in military settings. Following thawing, cryopreserved platelets are activated, resulting in faster clot formation but reduced aggregation in vitro, rendering their efficacy in bleeding unknown. Also, concerns remain on the safety of these products. The aim was to investigate the efficacy and safety of cryopreserved platelets in a rat model of traumatic hemorrhage.
Study Design and Methods: After 1 hour of shock, rats (n = 13/group) were randomized to receive a balanced transfusion pack (1:1:1 red blood cell:plasma: platelet) made from syngeneic rat blood, containing either liquid stored platelets or cryopreserved platelets. Primary outcome was the transfusion volume required to obtain a mean arterial pressure (MAP) of 60 mmHg. Secondary
Sources of support: Stichting Ziektekostenverzekering Krijgsmacht (SZVK) and the Dutch Ministry of Defense. DOI: 10.1111/trf.15937
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
© 2020 The Authors. Transfusion published by Wiley Periodicals LLC. on behalf of AABB.
outcomes were coagulation as assessed by thromboelastometry (ROTEM®) and organ failure as assessed by biochemistry and histopathology.
Results: The transfusion volume to obtain a MAP of 60 mmHg was lower in animals receiving cryopreserved platelets (5.4 [4.1-7.1] mL/kg) compared to those receiving liquid stored platelets (7.5 [6.4-8.5] mL/kg, p < 0.05). ROTEM® clotting times were shorter (45 [41-48] vs. 49 [45-53]sec, p < 0.05), while maxi-mum clot firmness was slightly lower (68 [67-68] vs. 69 [69-71]mm, p < 0.01). Organ failure was similar in both groups.
Conclusions: Use of cryopreserved platelets required less transfusion volume to reach a targeted MAP compared to liquid stored platelets, while organ injury was similar. These results provide a rationale for clinical trials with cryopreserved platelets in (traumatic) bleeding.
1
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I N T R O D U C T I O N
Trauma-induced coagulopathy is characterized by platelet dysfunction.1,2 Whereas platelet counts can be preserved during traumatic bleeding, platelet dysfunction occurs in approximately 45% of trauma patients.1-3 In accordance, transfusion of high doses of platelets results in a reduction in early death following trauma compared to lower doses of platelets.4,5 Liquid stored platelet products however, have a limited shelf-life (5-7 days at room temperature). Cryopreservation of platelets increases the lifespan of these products from days to years, rendering cryopreserved platelets suitable for use in austere and military environ-ments.6Following thawing, cryopreserved stored platelets are activated and show impaired aggregation and adhesion in vitro.7Also, recovery in vivo following autologous trans-fusion of thawed cryopreserved platelets is reduced com-pared to fresh autologous platelet products in healthy volunteers.8However, despite these observations, initiation of clot formation occurs faster and fibrin formation is unaf-fected.9Cryopreserved platelet products have been used in military and civilian settings, and in terms of clinical out-come, appear to have a similar performance compared to other platelet products.6,10-12 Despite these findings and the fact that cryopreservation could potentially resolve problems with availability or waste of platelet products, widespread use of cryopreserved platelets is hampered, which is probably due to a perceived loss of function of the platelets.7,13-15However, impaired aggregation in vitro and a reduced recovery in vivo do not correlate with the hemo-static potential of cryopreserved platelets.11 In contrast, cryopreserved platelets induce a more rapid hemostatic control compared to standard stored products in vitro, pre-sumably as a result of activation, a high platelet-derived extracellular vesicle content and an increased thrombin generating capacity.16In addition to questions relating to
the ability of cryopreserved platelet to control bleeding, questions concerning their safety remain. The advantage of the freeze-thawing-induced activation of the platelets for controlling bleeding may also have the disadvantage of an increased risk of thromboembolic events.17 Further-more, cryopreserved platelets have been shown to have immune-modulating effects in vitro and to augment a pro-inflammatory response with ensuing organ injury, as observed in mice.18
The aim of this study is to compare the hemostatic capacity of cryopreserved with liquid stored platelets in a rat model of traumatic hemorrhagic shock and to investi-gate the impact on organ injury. We hypothesized that resuscitation with cryopreserved platelets requires less volume to restore hemostasis and shock when compared to liquid stored platelets.
2
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M A T E R I A L S A N D M E T H O D S
2.1
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Ethics, species and intervention
This study was approved by the Institutional Animal Care and Use Committee of the Amsterdam University Medical Centers, location Academic Medical Center. The proce-dures were performed in accordance with the European Parliament directive (2010/63/EU) and the national law the Experiments on Animals Act (Wod, 2014). Animals were group housed (2 to 4 rats per cage) with access to water and food (2016 Teklad global 16% protein, Envigo, USA) ad libitum at least 7 days before the experiment. The light-dark cycle was from 7AMuntil 7PM. Experiments began at 8AM,
traumatic shock was completed around 10AMand ended at
4PM. A total 26 male Sprague Dawley rats weighing 350-400
grams (Envigo, UK) were subjected to a model of multiple trauma with uncontrolled liver bleeding.
2.2
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Experimental model
2.2.1
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Blood component manufacturing
methods
Forty syngeneic donor rats were used for the preparation of blood products as described before.19,20In short, whole blood was obtained through cardiac puncture and pre-pared and stored according to national blood bank stan-dards. Whole blood was mixed in a 9-to-1 ratio with citrate-phosphate-dextrose solution, after which blood was immediately centrifuged (10 min, 1892G, 20°C) to separate the blood in three different components. Most plasma was removed and stored at−80°C for 1 day. Two buffy coats were removed and diluted with the rest of plasma until a hematocrit of 20% was obtained. Thereaf-ter, to remove remaining red blood cells and leukocytes, the plasma diluted pooled buffy coat was centrifuged (10 min, 300G, 22°C) and platelet-rich supernatant plasma was obtained. Platelet-rich plasma was either kept on a roller bank in a temperature-controlled stove at 22°C to be used in the next 2 days or was further processed to cryopreserved platelets. The remaining (buffy coat removed) red blood cells were diluted to a hematocrit of 60% with additive solution (saline adeno-sine glucose mannitol SAGM) and stored at 4°C to be used the next day. One day after blood component pro-duction and storage, the products were (thawed and) used for transfusion.
The process to manufacture small volumes cryopreserved platelets was developed by the Dutch mili-tary blood bank, mimicking the procedure for human cryopreserved platelets.21-24 Dimethylsulfoxide (DMSO) 27% in saline (BloodStor® 27 NaCl Biopreservation Media; Biolife solutions Bothell, WA, USA) was added to fresh rat platelet-rich plasma in four equal steps (30 sec between steps) while gently stirring to a final DMSO con-centration of 6%. Next, this product was centrifuged (10 min, 1250G, 22°C, acceleration 9, brake 0, Eppendorf 4904R). Supernatant was removed (150μL was left on the pellet) and the pelleted platelets of the product were suspended during 1 minute with slow pipetting move-ments. To lower the freezing rate, which makes the freez-ing process comparable to human products, the product-tube was first wrapped in tissue paper in such a way that the wrapped tube fits in a 50 mL falcon tube. Thereafter, the package was placed upright in an−80°C freezer. The platelets were kept at −80°C before use. On the day of use, cryopreserved platelets were unwrapped and thawed for 5 minutes in a 37°C water bath, after which platelets were suspended with slow pipetting movements for 30 seconds while the tube was still in the water bath. Warm (35-37°C) thawed plasma product was added
rapidly to the suspended platelet pellet while the tube was mixed on a vortex in order to reconstitute the cryopreserved platelet product to the same volume of plasma as the liquid stored rat platelets. The thawed suspended rat platelets were used within 15 minutes after preparation.
When this process was piloted with small volume cryopreserved human platelets, it resulted in >80% in vitro recovery, which was comparable to recovery of standard volume cryopreserved human platelet products (data not shown). Also, the in vitro thromboelastography coagula-tion characteristics of small volume cryopreserved human platelets were comparable to that of normal volume cryopreserved human platelet products (data not shown).
2.2.2
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Model of traumatic bleeding
Animals received induction anesthesia with ketamine (Alfasan, The Netherlands), dexmedetomidine (Orion Pharma, Finland) and atropine (Dechra, The Nether-lands) and maintenance anesthesia with ketamine and dexmedetomidine intravenously. A tracheostomy was performed and rats were connected to a mechanical ven-tilator (Babylog 8000, Draeger, Germany). Pressure-con-trolled ventilation was applied with respiratory rate set at 60/min, a positive end expiratory pressure of 3.5 kPa and inspiratory pressures of 10 kPa, yielding tidal volumes between 7-8 mL/kg. Recruitment was performed every hour by increasing inspiratory pressures (Pinsp) to 25 kPa for 5 seconds. Respiratory rate was increased to 75/min during traumatic hemorrhagic shock. In case of a high PCO2 (>35 mmHg) with a low pH (<7.3), Pinsp was increased by 2 kPa. Monitoring of arterial blood pressure and blood sampling was done via an arterial catheter placed in the right carotid artery. The right jugular vein was cannulated and used for transfusion. Temperature was monitored with a rectal thermometer and kept between 36.5-37.0°C using a heat table and heat lamp.
Traumatic injury was inflicted by a fracture of the right femur employing a guillotine. Following a median laparotomy, crush injury of the small intestine was inflicted by clamping the gut five times approximately 2 cm from the Treitz ligament with 0.2 cm in-between the injuries. Isovolumic hemodilution was done with Ringerʼs Lactate (Baxter, USA) according to the formula (0.30(0.06× weight + 0.770).25 The liver was punctured at the left lateral lobe using a stance to penetrate a cir-cumference of 0.5 cm of the liver, leading to uncontrolled bleeding. The episode of uncontrolled bleeding lasted for 15 minutes with an open abdomen. If blood pressure did not drop below a mean arterial pressure (MAP) of 40 mmHg, a maximum of 1.5 mL of blood (in addition to
the isovolumic hemodilution) was drawn from the carotid artery line (controlled hemorrhage). If MAP dropped below 30 mmHg within the 15 minutes of uncontrolled bleeding period, the liver was packed with gauzes. After 15 minutes, the abdomen was closed to maintain adequate body temperatures. Total hemorrhage was the sum of controlled blood loss (baseline sample + maximum 1.5 mL during shock) and uncontrolled blood loss (estimation of blood loss in the abdomen). After a total shock duration of 1 hour (15 min uncon-trolled bleeding +45 min of MAP<40 mmHg), rats were randomized to receive resuscitation with a 1:1:1 volume ratio of red blood cell:plasma:liquid stored platelets (liq-uid stored) or 1:1:1 volume ratio of red blood cell:plasma: cryopreserved platelets (cryopreserved). Transfusion was set at a speed of 8.0 mL/hour. After reaching a MAP of 60 mmHg for 5 minutes, transfusion was stopped. Thirty minutes before termination of the experiment (at 5.5 hours), a FITC-labeled 70 kDa dextran was adminis-tered to assess endothelial barrier leakage. After euthanization by bloodletting, the circulation was flushed against gravitational force with 50 mL NaCl 0.9%. Both vascular supply of the left lung and left kidney were tied-off during this process to assess wet/dry ratios of these organs. Wet weight was measured by measuring the weight of the left lung/kidney, drying the organ for 1 week at 60°C, and reevaluating the weight of the dried organ.
2.2.3
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Measurements during the
experiment
Blood samples were obtained just before trauma (T0), after 1 hour of shock and just before initiation of transfu-sion (T1), at 3 hours (T3), at 4 hours (T4) and after 6 hours at termination of the experiment and subsequent euthanization of the animals (T6). Blood was assessed for arterial blood gas and electrolytes at all time points and rotational thromboelastometry (ROTEM® Delta, Werfen, Spain) at four time points (T0, T1, T3, and T6). Thrombo-cyte count (XN-9000, Sysmex, Japan), hemoglobin/ hematocrit (RAPIDPoint 500, Siemens Healtineers, Ger-many), prothrombin time and Clauss fibrinogen level (CS2500, Siemens Healthineers, Germany), aspartate trans-aminase, alanine transaminases, creatinine (Cobas c702, Roche, Switzerland) and urine protein (Cobas c502, Roche, Switzerland) were measured at two time points (T0, T6).
2.2.4
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Rotational thromboelastometry
The EXTEM assay evaluates the extrinsic coagulation pathway, using tissue factor and phospholipids to initiate coagulation. Clotting time (CT) determines time to clot
initiation, the alpha angle assesses the rate of clot forma-tion, maximum clot firmness (MCF) represents the strength of the clot and the 30 minutes lysis index shows the percentage of amplitude decrease 30 minutes after maximum clot firmness, indicating clot lysis. The FIBTEM assay uses EXTEM initiators of coagulation plus a potent platelet inhibitor (cytocholasin D) to eliminate platelet contribution to evaluate the contribution of fibrinogen to clot formation. To assess the platelet com-ponent of clot formation, the FIBTEM MCF value is sub-tracted from the EXTEM MCF value.
2.2.5
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Enzyme-linked immunosorbent
assays (ELISA)
Levels of circulating syndecan-1, a component of the endothelial glycocalyx, and high mobility group protein B1 (HGMB-1),26damage marker released from predomi-nantly platelets, were measured with ELISAs according to manufacturerʼs guidelines (eLabscience, USA).
2.2.6
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Organ assessments
The hematoxylin and eosin slides of the lung, liver, spleen, small intestine, and kidney were scored by a pathologist, who was blinded to treatment allocation. This scoring sys-tem has been used before.19,20The lung, for example, was scored based on lung edema, interstitial inflammatory cell infiltration, endothelialitis, and hemorrhage. The scale of each category consisted of a score of 0 (=absent) to 3 (=severe). For the full scoring list see Table S1, available as supporting information in the online version of this paper.
2.2.7
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Immunostaining FITC-dextran
leakage
Deparaffinized blanco organ slides of the lung and kidney were colored using a rabbit - anti-FITC/anti-rabbit horse radish peroxidase and NovaRed coloring method. The stop-ping times were kept constant for all slides. Five different images of each organ, blinded for the treatment allocation to the assessor, were obtained with microscope (10x zoom) and camera (BX51 with UC90, Olympus, Japan). Pictures were inverted using Image J. Five random inverted pictures were used to set a threshold indicating presence of FITC-70 kDa dextran leakage. Median percentage of area inten-sity was used as measure for endothelial leakage.
2.3
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Sample size calculation
Based on previous experiments,19given a treatment effect of 0.6 mL/kg and a standard deviation of 0.47 mL/kg, 11
rats per group have a power of 80% to detect a statistical significant difference in transfusion volume needed to reach a MAP of 60 mmHg. Because we previously experi-enced a mortality of 20% in our model, we added two additional rats per group, yielding 13 per experimental group.
2.4
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Statistical analysis
Data were analyzed using SPSS (IBM, version 25.0), graphs were made using GraphPad Prism (version 8.0.2). All parameters were first assessed for distribution and checked for normality using a Kolmogorov-Smirnov test and by visual inspection of histograms. Data were pres-ented based on their distribution as median with inter-quartile range, mean with standard deviation or percentage. Parameters were tested for differences using the Mann-Whitney U test, Student T test, or Chi-Squared test. Paired (T0 vs. T6) nonparametric differences were tested within groups with a Friedman ANOVA. A p value of less than 0.05 was considered statistically significant.
3
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R E S U L T S
3.1
|
Trauma, shock, and transfusion
needs
Traumatized animals were in severe shock in both groups, indicated by high base deficits, increased lactate
levels and low blood pressures without significant differ-ences between group (Table 1, Fig. 1). Controlled blood loss (baseline sample + additional bloodletting) plus esti-mated uncontrolled blood (estiesti-mated volume of blood loss in the abdomen) loss during the shock period were not different between cryopreserved and liquid stored platelet treated rats (total blood loss of 9.6 [8.8-10.1] vs. 9.7 [9.0-10.3] mL, p = 0.84). All animals survived the 6-hour time point.
Quality assessments of the different blood products are described in the Table S2, available as supporting information in the online version of this paper. The rat cryopreserved platelet product yielded a median in vitro freeze-thaw recovery of 87% [69-100]. The volume of transfusion needed to restore circulation to the pre-determined MAP of 60 mmHg was significantly lower in the cryopreserved platelet transfused rats compared to the liquid stored platelet transfused rats (5.4 [4.1-7.1] mL/kg vs. 7.5 [6.4-8.5] mL/kg, p = 0.02). The degree of shock as assessed by lactate levels and base deficits was similar in both groups. These variables remained similar between groups over the course of the experiment.
3.2
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Coagulation
Our trauma and shock model resulted in decreased plate-let counts, prolonged prothrombin time and decreased fibrinogen levels, without differences between groups. Thrombocyte counts were equal also at the end of the experiment (Table 2). Both groups remained coagulopathic
T A B L E 1 Parameters at baseline, after traumatic shock and after resuscitation strategy
Liquid stored platelets Cryopreserved platelets
Parameter Before injury (T0) After injury and shock (T1) After transfusion (T3) Before injury (T0)
After injury and shock (T1) After transfusion (T3) Weight (gram) 359 (344-373) ND ND 346 (339-366) ND ND pH 7.39 (7.37-7.45) 7.41 (7.37-7.43) 7.41 (7.37-7.42) 7.43 (7.39-7.47) 7.39 (7.32-7.45) 7.40 (7.36-7.42) pCO2(mmHg) 34.9 (31.0-41.4) 24.9 (23.8-27.4) 28.8 (26.2-30.1) 36.5 (33.9-38.9) 23.8 (21.2-32.1) 28.3 (23.4-32.3) BE (mEq/L) −0.7 (−2.3-0.1) −8.0 (−8.6-−6.8) −6.0 (−8.3-−5.6) 0.0 (−2.0-1.6) −8.0 (−11.0 - −6.0) −7.3 (−8.2 - −6.1) Lactate (mmol/L) 0.7 (0.6-0.8) 3.7 (3.1-4.9) 2.3 (2.0-2.9) 0.7 (0.6-0.7) 3.8 (2.8-7.4) 2.1 (1.6-3.4) Na+(mmol/L) 139 (138-140) 130 (128-134) 137 (135-140) 139 (138-141) 131 (129-132) 138 (136-139) K+(mmol/L) 4.1 (3.9-4.6) 5.9 (5.7-6.8) 5.8 (5.4-6.1) 4.1 (3.9-4.3) 6.3 (6.0-6.7) 5.7 (5.3-6.0) Ca2+(mmol/L) 1.0 (1.0-1.1) 1.0 (0.9-1.1) 1.1 (1.0-1.2) 1.1 (1.1-1.1) 1.1 (1.0-1.1) 1.1 (1.0-1.1) Cl−(mmol/L) 107 (105-108) 104 (100-108) 107 (106-112) 107 (105-108) 104 (101-107) 109 (108-111) Glucose (mmol/L) 18.4 (17.1-20.1) 31.3 (29.9-36.6) 22.5 (19.8-24.7) 17.6 (17.3-18.8) 34.7 (30.4-35.5) 20.1 (17.9-21.3) Note:Data are presented as median (IQR).
after trauma and resuscitation, as shown by approximately 1.3 times prolonged prothrombin times compared to base-line, without differences between the cryopreserved (13.9 [12.2-14.4] sec) and the liquid stored platelet treated group (14.2 [12.7-15.8] sec, p = 0.36). Also, fibrinogen levels remained low in both groups 6 hours post injury, without differences in the cryopreserved platelet group (1.3 [1.1-1.6] g/L) compared to the liquid stored platelet group (1.3 [1.0-1.4] g/L, p = 0.34). The ROTEM® assays were mea-sured at multiple time points (Fig. 2). Trauma, blood loss, and saline dilution reduced FIBTEM clot strength but did not significantly affect EXTEM clot strength or clotting times within 1 hour after trauma. Two hours following transfusion, EXTEM clotting time was signifi-cantly shorter in the cryopreserved platelet treated rats (45 [41-48] sec) compared to the liquid stored platelet group (49 [45-53] sec, p < 0.05), while maximum clot firmness was slightly but significantly decreased (68 [67-68] mm vs. 69 [69-71] mm, p < 0.01). The platelet con-tribution to clot formation was similar between the cryopreserved group compared to the liquid stored platelet group (57 [55-57] mm vs. 59 mm [54-60], p = 0.06). There was no lysis present during this experi-ment in both groups.
3.3
|
Organ injury
Trauma resulted in acute lung, acute kidney, and acute liver injury (Table 2, Fig. 3). Lung injury did not reveal differences between cryopreserved and liquid stored platelet treated rats, depicted by similar lung wet/dry ratios (5.5 [5.2-5.7] vs. 5.2 [4.7-5.6], p = 0.22) and similar lung histology scores (Fig. 3). Kidney injury was not dif-ferent, with similar creatinine levels and kidney wet/dry ratios in the cryopreserved platelet (4.3 [3.9-4.7]) vs. liq-uid stored platelets (4.3 [3.7-4.6], p = 0.88). In addition, groups did not differ in leakage of FITC-dextran from the circulation into the lung and kidney (Table 2). Syndecan-1, a marker for glycocalyx degradation, was elevated after trauma, but was not different between groups. Thereby, cryopreserved platelets compared to liquid stored plate-lets had no impact on endothelial permeability. Also, liver injury did not differ between groups, as determined by similar ALT (alanine transaminase) levels. Assessing organ histology scores revealed no differences between groups (Fig. 3). Thrombus formation was only observed on the site where injury was directly inflicted, without differences between groups. No thrombi were observed in organs without direct traumatic injury. Individual scores
F I G U R E 1 Shock and resuscitation needs. Data are median with interquartile ranges. (A) Mean arterial pressure. Between T0 and T1: 1 hour shock phase; between T1 and T2: transfusion phase. Three hours,34 hours,4and 6 hours6after trauma additional blood samples were taken. (B) Transfusion until MAP 60 mmHg. (C) Lactate. (D) Base excess. Rats were treated with either a balanced 1:1:1 red blood cell: plasma:platelet with liquid-stored platelets or a balanced transfusion ratio with cryopreserved platelets. Dotted vertical line represents when resuscitation was initiated. *p < 0.05 between groups
of the different organs are shown in Fig. S1, available as supporting information in the online version of this paper. HMGB-1 is a damage molecule that is released from platelets. The level of HMGB-1 was markedly ele-vated after traumatic shock, however there were no sig-nificant differences between the liquid stored platelet group and the cryopreserved platelet group.
4
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D I S C U S S I O N
In this model of uncontrolled traumatic bleeding, a bal-anced transfusion strategy containing cryopreserved platelets required 28% less blood product volume to reach a targeted MAP when compared to a strategy using liq-uid-stored platelets. Reduced transfusion needs were associated with a faster initiation of clot formation as assessed by ROTEM®, but lower clot amplitude. Use of cryopreserved platelets was comparable to treatment with liquid stored platelets in terms of organ injury.
In our model, the lower volume of transfusion needed to restore MAP to a predefined target in the cryopreserved platelet treated rats, may be attributed to the faster clotting times that were observed with ROTEM®. These data are in line with previous in vitro
data, that showed that cryopreserved platelets reduced clotting times compared to liquid stored platelets.27-29 The reason why cryopreserved platelets compared to liq-uid stored platelets reduce ROTEM clotting times might be due to increased procoagulant microparticle content and increased thrombin generation.16,30 We found that clot firmness was slightly reduced in the cryopreserved platelet group, although this effect was smaller than found in previous in vitro studies.7,9,16Reduction in clot firmness most likely was not due to lower fibrinogen activity, as fibrinogen levels as well as ROTEM® FIBTEM did not differ between groups. Thereby, the reduction in clot strength in the cryopreserved group may be due to reduced platelet function. In line with this, results of the MCF EXTEM minus FIBTEM were also lower in the cryopreserved platelet group when compared to the liq-uid platelet group. The differences in clot firmness were however very small (median difference of 1 mm) and it is not clear whether this reflects clinical relevance. Our data suggest that a balanced transfusion with cryopreserved platelets is possibly better for achieving hemostasis com-pared to liquid stored platelets, even when clot firmness is somewhat reduced. In line with this, cryopreserved platelets formed similar amounts of fibrin in in vitro flow models compared to liquid stored platelets,21which also
T A B L E 2 Coagulation, endothelial leakage, and biochemical assessment of organ injury
Parameter
Liquid stored platelets Cryopreserved platelets
Before injury (T0) After 6 hours (T6) Before injury (T0) After 6 hours (T6) Hemoglobin (mmol/L) 9.2 (8.9-9.4) 6.3 (5.7-6.5) 9.0 (8.6-9.6) 6.4 (5.8-6.6) Hematocrit (%) 44 (42-44) 30 (27-31) 43 (41-46) 30 (27-31) Coagulation and HMGB-1 Thrombocytes (*109/L) 975 (917-998) 511 (399-654)** 904 (832-1003) 448 (376-509)** Fibrinogen (g/L) 2.3 (2.1-2.4) 1.3 (1.0-1.4)** 2.2 (2.1-2.4) 1.3 (1.1-1.6)** PT (sec) 10.8 (10.6-10.9) 14.2 (12.7-15.8)** 10.7 (10.5-10.9) 13.9 (12.2-14.4)** HMGB-1 (ng/mL) 1.4 (1.3-1.8) 25.5 (13.5-33.1)** 1.5 (1.3-1.6) 21.5 (10.2-26.1)** Endothelial leakage Syndecan-1 (ng/mL) 61.0 (42.7-106.6) 136.6 (108.7-173.1)** 54.9 (46.5-64.4) 105.1 (86.4-150.8)**
Area FITC leakage-lung (%) NA 13.2 (7.0-20.0) NA 14.3 (9.5-18.0)
Area FITC leakage-kidney (%) NA 20.0 (13.4-28.6) NA 25.6 (20.7-29.8)
Biochemical assessment of organ injury
ALT (U/L) 49.5 (44.3-53.5) 1315.0 (872.0-1822.0)** 52.0 (48.5-57.5) 1093.0 (685.0-1635.0)** AST (U/L) 58.0 (54.0-65.0) 2733.0 (1436.5-3598.5)** 61.0 (57.0-63.0) 1656 (1123.0-3276.0)** Creatinine (μmol/L) 24.0 (24.0-26.5) 142.0 (104.5-156.5)** 24.0 (23.0-25.5) 145.0 (128.0-155.0)** Urine protein (g/L) 0.6 (0.4-1.0) 1.7 (1.3-1.9) * 0.9 (0.7-1.0) 1.7 (1.6-2.2)*
Note:Data are presented as median (IQR). *p < 0.05 within group (T0-T6), **p < 0.01 within group (T0-T6). No significant between group differences were detected.
Abbreviations: ALT, alanine transaminase; AST, aspartate transaminase; FITC, fluorescein isothiocyanate; HMGB-1, high mobility group protein B1; NA, not applicable; PT, prothrombin time.
suggests that decreased in vitro platelet functions of cryopreserved platelets such as clot strength, aggregation, and adhesion may not be clinically relevant to reduce bleeding in vivo.
Clinical data comparing the efficacy of cryopreserved platelets to liquid stored platelets in patients are sparse. In an older cardiac surgery trial, cryopreserved platelet transfusion resulted in less blood loss and less blood product use compared to liquid stored platelets.11 This result was however not reproduced in a more recent pilot
trial in cardiac surgery patients, in which no difference in blood loss was shown between groups.12 Notably, patients treated with liquid stored platelet were twice more likely to have a postoperative bleeding compared to patients treated with cryopreserved platelets.12 In obser-vational studies in trauma patients, the efficacy of cryopreserved platelets was comparable to historical con-trols treated with liquid stored platelets.10 Our data add to the rationale of designing a follow-up trial investigat-ing efficacy. 6 0 30 40 50 60 Second s EXTEM A B C D E F G H CT * 6 0 30 40 50 60 Second s FIBTEM CT 0 30 40 50 60 70 80 90 degree s EXTEM alpha 0 30 40 50 60 70 80 90 degree s FIBTEM alpha 6 0 40 60 65 70 75 80 mm EXTEM MCF ** 6 0 5 10 15 mm FIBTEM MCF 6 0 40 40 50 60 mm EXTEM - FIBTEM MCF 0 1 2 3 4 5 0 1 2 3 4 5 0 1 2 3 4 5 6 0 1 2 3 4 5 6 0 1 2 3 4 5 0 1 2 3 4 5 0 1 2 3 4 5 0 1 2 3 4 5 6 0 50 100 % EXTEM Li30
Liquid stored Cryopreserved
F I G U R E 2 Rotational thromboelastometry. Data are represented as median with interquartile ranges. (A) EXTEM clotting time. (B) FIBTEM clotting time. (C) EXTEM alpha angle. (D) FIBTEM alpha angle. (E) EXTEM maximum clot firmness. (F) FIBTEM maximum clot firmness. (G) EXTEM MCF subtracted by FIBTEM MCF, depicting the platelet contribution to maximum clot firmness. (H) EXTEM lysis index at 30 minutes post maximum clot firmness. Dotted vertical line represents when resuscitation was initiated. *p < 0.05, **p < 0.01 between groups
In terms of safety, we found no significant differences in endothelial leakage, edema, or organ injury between groups. Previously, in a mouse model of controlled bleeding, use of cryopreserved platelets was associated with high ALT levels, hepatic macrophage infiltration, and hepatic myeloperoxidase activity compared to liquid stored platelet treated mice.31 An explanation for these different results may be the use of a different transfusion model. In the pre-sent study, cryopreserved platelets in plasma were adminis-tered in addition to red blood cells, whereas only platelets in plasma were transfused in the mouse model.31 Further-more, HMGB-1 levels were not different between groups in this study. Damaged cells and platelets release HMGB-1. HMGB-1 acts as an alarmin and is positively correlated with neutrophil activation, thrombosis and organ failure in trauma.17,32-34 We found no evidence that cryopreserved platelets resulted in HMGB-1-mediated inflammation.
The current model has some limitations. This study was designed employing a pressure-fixed transfusion tar-get as primary outcome. The group of cryopreserved platelets required less transfusion volume compared to liquid stored platelet group. As transfusion is associated with organ injury, we cannot exclude that transfusion of equal volumes would have resulted in higher organ injury scores in the cryopreserved group. However, in clinical practice, a pressure-fixed target is commonly used
as resuscitation goal to minimize transfusion. The resusci-tation target of 60 mmHg was chosen based on a previous study in which a target of 60 mmHg compared to other targets did not result in increased mortality, did not increase interleukin levels, reduced blood loss and reduced amount of fluid therapy.35Furthermore, rats differ in their coagulation system compared to humans, including higher ranges of platelet counts, hampering translation to humans.36However, similar to humans, rats also encoun-ter a platelet dysfunction due to traumatic shock.37
In conclusion, transfusion of cryopreserved platelets in a rat trauma transfusion model results in improved clotting time and reduced blood transfusion requirements. In terms of organ injury, cryopreserved platelets appear to be as safe as liquid stored platelets. The results provide a rationale for clinical studies investigating the efficacy and safety of cryopreserved platelets in traumatic bleeding. C O N F L I C T O F I N T E R E S T
The authors have disclosed no conflicts of interest. O R C I D
Derek J.B. Kleinveld https://orcid.org/0000-0002-6357-1471
Tim W.H. Rijnhout https://orcid.org/0000-0002-2736-5101
F I G U R E 3 Organ histology scores. Data are presented as boxplot with total range. Cumulative scores of the (A) lung, (B) kidney, (C) liver, and (D) small intestine are shown. For individual scores and total spleen score: see Fig. S1, available as supporting information in the online version of this paper
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S U P P O R T I N G I N F O R M A T I O N
Additional supporting information may be found online in the Supporting Information section at the end of this article.
How to cite this article: Kleinveld DJB, Sloos PH, Noorman F, et al. The use of cryopreserved platelets in a trauma-induced hemorrhage model. Transfusion. 2020;60: 2079–2089.https://doi.org/10.1111/trf.15937
